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Naotaka Tsutsumi

Advanced Institute of Industrial Technology ·
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Area of research
Molecular Biology · Computational Theory and Mathematics
Research interest
Research interests include Computational Drug Discovery Methods, Cytokine Signaling Pathways and Interactions, Heat shock proteins research, and Monoclonal and Polyclonal Antibodies Research.
h-index
19
citations
1,520
works
62
NIH funding
primary concept
email

Recent publications

Structural basis of Janus kinase trans-activation
Cell Reports 2023cited by 49position: middledoi
Structure of the thrombopoietin-MPL receptor complex is a blueprint for biasing hematopoiesis
Cell 2023cited by 42position: firstdoi
Structural insight into guanylyl cyclase receptor hijacking of the kinase–Hsp90 regulatory mechanism
eLife 2023cited by 7position: middledoi
Structural insight into guanylyl cyclase receptor hijacking of the kinase–Hsp90 regulatory mechanism
eLife 2023cited by 5position: middledoi
Structure of a Janus kinase cytokine receptor complex reveals the basis for dimeric activation
Science 2022cited by 172position: middledoi
Organizing structural principles of the IL-17 ligand–receptor axis
Nature 2022cited by 77position: middledoi
Atypical structural snapshots of human cytomegalovirus GPCR interactions with host G proteins
Science Advances 2022cited by 41position: firstdoi
Viral G Protein–Coupled Receptors Encoded by β- and γ-Herpesviruses
Annual Review of Virology 2022cited by 39position: middledoi
Structure of the IL-27 quaternary receptor signaling complex
eLife 2022cited by 38position: middledoi
Structure-based decoupling of the pro- and anti-inflammatory functions of interleukin-10
Science 2021cited by 221position: middledoi
Structural basis for the constitutive activity and immunomodulatory properties of the Epstein-Barr virus-encoded G protein-coupled receptor BILF1
Immunity 2021cited by 38position: firstdoi
Structure of human Frizzled5 by fiducial-assisted cryo-EM supports a heterodimeric mechanism of canonical Wnt signaling
eLife 2020cited by 141position: firstdoi
Structure and selectivity engineering of the M <sub>1</sub> muscarinic receptor toxin complex
Science 2020cited by 59position: middledoi
Structure of the IFNγ receptor complex guides design of biased agonists
Nature 2019cited by 137position: middledoi
Viral GPCR US28 can signal in response to chemokine agonists of nearly unlimited structural degeneracy
eLife 2018cited by 61position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

K. Christopher García · Tecnológico de Monterrey15 papers (2018–2023)Kevin M. Jude · Stanford University8 papers (2018–2023)Nathanael A. Caveney · University of British Columbia6 papers (2022–2023)Deepa Waghray · Stanford University5 papers (2018–2023)Robert A. Saxton · University of California, Berkeley3 papers (2021–2023)Brian K. Kobilka · Stanford University3 papers (2020–2022)Jacob Piehler · North Carolina State University3 papers (2019–2023)Shoji Maeda · University of Michigan–Ann Arbor3 papers (2020–2022)Caleb R. Glassman · Stanford University3 papers (2022–2023)Cornelius Gati · University of Southern California3 papers (2020–2023)Mette M. Rosenkilde · University of Copenhagen3 papers (2018–2022)Qianhui Qu · Fudan University2 papers (2021–2022)Steven C. Wilson · University of California, Berkeley2 papers (2022–2023)John S. Burg · Io Therapeutics (United States)2 papers (2018–2020)Georgios Skiniotis · Stanford Medicine2 papers (2021–2022) · 2 papers (2020–2021)Leon Su · Mayo Clinic Hospital2 papers (2019–2021)Robert S. Haltiwanger · University of Georgia1 papers (2019–2019) · 1 papers (2022–2022) · 1 papers (2019–2019)
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